EP2467858B1 - Polykristalline magnetokalorische materialien - Google Patents
Polykristalline magnetokalorische materialien Download PDFInfo
- Publication number
- EP2467858B1 EP2467858B1 EP10744924.1A EP10744924A EP2467858B1 EP 2467858 B1 EP2467858 B1 EP 2467858B1 EP 10744924 A EP10744924 A EP 10744924A EP 2467858 B1 EP2467858 B1 EP 2467858B1
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- EP
- European Patent Office
- Prior art keywords
- magnetocaloric
- solid
- mol
- cooling
- replaced
- Prior art date
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- 239000000463 material Substances 0.000 title claims description 54
- 238000001816 cooling Methods 0.000 claims description 29
- 238000005245 sintering Methods 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims description 15
- 239000012071 phase Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 229910045601 alloy Inorganic materials 0.000 claims description 10
- 239000000956 alloy Substances 0.000 claims description 10
- 238000002074 melt spinning Methods 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 229910052748 manganese Inorganic materials 0.000 claims description 8
- 239000012298 atmosphere Substances 0.000 claims description 7
- 238000010791 quenching Methods 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 6
- 230000000171 quenching effect Effects 0.000 claims description 6
- 239000007791 liquid phase Substances 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 239000011261 inert gas Substances 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 239000007790 solid phase Substances 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 3
- 239000007769 metal material Substances 0.000 claims description 3
- 229910052729 chemical element Inorganic materials 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 229910015335 Ni2In Inorganic materials 0.000 claims 1
- 238000003825 pressing Methods 0.000 claims 1
- 230000005291 magnetic effect Effects 0.000 description 30
- 230000000694 effects Effects 0.000 description 20
- 239000010949 copper Substances 0.000 description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 9
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- 238000003746 solid phase reaction Methods 0.000 description 5
- 108010053481 Antifreeze Proteins Proteins 0.000 description 4
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 229910052796 boron Inorganic materials 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
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- 238000012546 transfer Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000238366 Cephalopoda Species 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000000333 X-ray scattering Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
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- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 229910001009 interstitial alloy Inorganic materials 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
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- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000005298 paramagnetic effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
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- 238000006467 substitution reaction Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/012—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials adapted for magnetic entropy change by magnetocaloric effect, e.g. used as magnetic refrigerating material
- H01F1/015—Metals or alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/07—Alloys based on nickel or cobalt based on cobalt
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C22/00—Alloys based on manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C30/00—Alloys containing less than 50% by weight of each constituent
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/012—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials adapted for magnetic entropy change by magnetocaloric effect, e.g. used as magnetic refrigerating material
- H01F1/017—Compounds
Definitions
- the invention relates to polycrystalline magnetocaloric materials, processes for their preparation and their use in coolers, heat exchangers or generators, in particular refrigerators.
- Thermomagnetic materials also referred to as magnetocaloric materials, can be used for cooling, for example, in refrigerators or air conditioners, in heat pumps, or for direct recovery of heat from power without the interposition of mechanical energy conversion.
- the magnetic cooling techniques are based on the magnetocaloric effect (MCE) and can be an alternative to the known steam-cycle cooling methods.
- MCE magnetocaloric effect
- the alignment of randomly oriented magnetic moments with an external magnetic field results in heating of the material. This heat can be dissipated from the MCE material into the ambient atmosphere by heat transfer.
- the magnetic field is then turned off or removed, the magnetic moments revert to a random arrangement, causing the material to cool to below ambient temperature.
- This effect can be used for cooling purposes, see also Nature, Vol. 415, 10 January 2002, pages 150 to 152 .
- a heat transfer medium such as water is used for heat removal from the magnetocaloric material.
- thermomagnetic generators are also based on the magnetocaloric effect.
- a material exhibiting a magnetocaloric effect the alignment of randomly oriented magnetic moments with an external magnetic field results in heating of the material. This heat can be dissipated from the MCE material into the ambient atmosphere by heat transfer. When the magnetic field is subsequently turned off or removed, the magnetic moments revert to a random arrangement, causing the material to cool to below ambient temperature. This effect can be exploited on the one hand for cooling purposes, on the other hand, to convert heat into electrical energy.
- Magnetocaloric generation of electrical energy is associated with magnetic heating and cooling.
- the method of energy production was described as pyromagnetic energy generation.
- these magnetocaloric devices can have significantly higher energy efficiency.
- a pyromagneto-electric generator is, for example, by N. Tesla in US 428,057 described. It is stated that the magnetic properties of iron or other magnetic substances can be partially or completely destroyed or disappear by heating to a certain temperature. Upon cooling, the magnetic properties are restored and return to the initial state. This effect can be exploited to generate electricity.
- an electrical conductor is exposed to a varying magnetic field, changes in the magnetic field will induce an electrical current in the conductor.
- the magnetic material is enclosed by a coil and then heated in a permanent magnetic field and subsequently cooled, an electrical current is induced in the coil in each case during the heating and cooling. As a result, heat energy can be converted into electrical energy without, in the meantime, converting into mechanical work.
- iron is heated as a magnetic substance via an oven or a closed hearth and subsequently cooled again.
- thermomagnetic or magnetocaloric applications the material should permit efficient heat exchange in order to achieve high efficiencies. Both in cooling and in power generation, the thermomagnetic material is used in a heat exchanger.
- the object of the present invention is to provide magnetocaloric materials having a large magnetocaloric effect.
- phase of the orthorhombic TiNiSi structure type and of the hexagonal Ni 2 In structure type are present at a temperature below -40 ° C.
- A may be boron or carbon.
- polycrystalline magnetocaloric materials in which both phases of the orthorhombic TiNiSi structure type and of the hexagonal Ni 2 In structure type are present exhibit an unexpectedly high magnetocaloric effect. They are almost intrinsically two-phase magnetocaloric materials. Of the two phases mentioned, the polycrystalline magnetocaloric materials preferably contain at least 5% by weight, more preferably at least 10% by weight, in particular at least 15% by weight.
- MnCoGe-type materials which are not stoichiometric and show either voids in the Ge sublattice or Fe, Ni, Cr, V, or Cu substitutions in the Co sublattice.
- MnCoGe structures formed by boron as interstitial atoms which are obtained by adding small amounts of boron to stoichiometric MnCoGe, show great magnetocaloric effects. The largest magnetocaloric effects are observed for interstitial alloys.
- the proportions of the phase transitions can be adjusted, which in turn the magnetic moments and the magnetocaloric effect can be adjusted.
- the materials Above the Curie temperature, the materials are usually single-phase, but below the Curie temperature two-phase.
- the intermetallic compound MnCoGe crystallizes in the orthorhombic TiNiSi structure type with a Curie temperature of 345 K.
- MnCoGe exhibits a typical second-order magnetic phase transition.
- the isothermal magnetic entropy change of MnCoGe is about 5 J kg -1 K -1 . It would have been expected that replacing Co with other elements would lower both the magnetic moment and the Curie temperature. According to the invention, however, it has been found that the possible structural transition from the orthorhombic TiNiSi structure type to the hexagonal Ni 2 In structure type leads to large magnetocaloric effects in the compounds.
- x has the value 0.01 to 0.05.
- Mn or Co is replaced as indicated, more preferably 1 to 20 mol%, especially 3 to 10 mol%.
- thermomagnetic materials used in the invention can be prepared in any suitable manner.
- the magnetocaloric materials of the present invention can be prepared by solid phase reaction or liquid phase reaction of the starting materials for the material, subsequent cooling, subsequent compression, sintering and annealing under an inert gas atmosphere followed by cooling to room temperature or by melt spinning a melt of the starting or starting alloys.
- thermomagnetic materials for example, by solid phase reaction of the starting elements or starting alloys for the material in a ball mill, subsequent compression, sintering and annealing under inert gas atmosphere and subsequent, z. Slow, cooling to room temperature.
- a method is for example in J. Appl. Phys. 99, 2006, 08Q107 described.
- Thermal hysteresis can be significantly reduced and a large magnetocaloric effect can be achieved if the metal-based materials are not slowly cooled to ambient temperature after sintering and / or annealing, but are quenched at a high cooling rate.
- the cooling rate is at least 100 K / s.
- the cooling rate is preferably 100 to 10,000 K / s, more preferably 200 to 1300 K / s. Especially preferred are cooling rates of 300 to 1000 K / s.
- the quenching can be achieved by any suitable cooling method, for example by quenching the solid with water or aqueous liquids, such as cooled water or ice / water mixtures.
- the solids can be dropped, for example, in iced water. It is also possible to quench the solids with undercooled gases such as liquid nitrogen. Other quenching methods are known to those skilled in the art.
- the advantage here is a controlled and rapid cooling.
- thermomagnetic materials The rest of the preparation of the thermomagnetic materials is less critical, as long as the quenching of the sintered and / or tempered solid takes place in the last step with the cooling rate according to the invention.
- the method can be applied to the production of any suitable thermomagnetic materials for magnetic cooling, as described above.
- step (a) of the method the reaction of the elements and / or alloys, which are contained in the later thermomagnetic material, in a stoichiometry, which corresponds to the thermomagnetic material, in the solid or liquid phase.
- the reaction in step a) is carried out by co-heating the elements and / or alloys in a closed container or in an extruder, or by solid-phase reaction in a ball mill.
- a solid phase reaction is carried out, which takes place in particular in a ball mill.
- powders of the individual elements or powders of alloys of two or more of the individual elements which are present in the later thermomagnetic material are typically mixed in powder form in suitable proportions by weight. If necessary, additional grinding of the mixture can be carried out to obtain a microcrystalline powder mixture.
- This powder mixture is preferably heated in a ball mill, which leads to a further reduction as well as good mixing and to a solid phase reaction in the powder mixture.
- the individual elements are mixed in the selected stoichiometry as a powder and then melted.
- the common heating in a closed container allows the fixation of volatile elements and the control of the stoichiometry. Especially with the use of phosphorus, this would easily evaporate in an open system.
- reaction is followed by sintering and / or tempering of the solid, wherein one or more intermediate steps may be provided.
- the solid obtained in step a) may be subjected to shaping before it is sintered and / or tempered.
- melt spinning processes are known per se and, for example, in Rare Metals, Vol. 25, October 2006, pages 544 to 549 as well as in WO 2004/068512 described.
- the composition obtained in step a) is melted and sprayed onto a rotating cold metal roller.
- This spraying can be achieved by means of positive pressure in front of the spray nozzle or negative pressure behind the spray nozzle.
- a rotating copper drum or roller is used which, if desired, may be cooled.
- the copper drum preferably rotates at a surface speed of 10 to 40 m / s, in particular 20 to 30 m / s.
- the liquid composition is cooled at a rate of preferably 10 2 to 10 7 K / s, more preferably at a rate of at least 10 4 K / s, in particular at a rate of 0.5 to 2 x 10 6 K / s.
- the melt spinning can be carried out as well as the reaction in step a) under reduced pressure or under an inert gas atmosphere.
- the Meltspinning a high processing speed is achieved because the subsequent sintering and annealing can be shortened. Especially on an industrial scale so the production of thermomagnetic materials is much more economical. Spray drying also leads to a high processing speed. Particularly preferably, the melt spinning (Melt spinning) is performed.
- a spray cooling may be carried out, in which a melt of the composition from step a) is sprayed into a spray tower.
- the spray tower can be additionally cooled, for example.
- cooling rates in the range of 10 3 to 10 5 K / s, in particular about 10 4 K / s are often achieved.
- the sintering and / or tempering of the solid takes place in stage c) preferably first at a temperature in the range from 800 to 1400 ° C. for sintering and subsequently at a temperature in the range from 500 to 750 ° C. for tempering.
- sintering may then take place at a temperature in the range of 500 to 800 ° C.
- shaped bodies / solids sintering is particularly preferably carried out at a temperature in the range from 1000 to 1300 ° C., in particular from 1100 to 1300 ° C.
- the tempering can then take place at 600 to 700 ° C, for example.
- the sintering is preferably carried out for a period of 1 to 50 hours, more preferably 2 to 20 hours, especially 5 to 15 hours.
- the annealing is preferably carried out for a time in the range of 10 to 100 hours, particularly preferably 10 to 60 hours, in particular 30 to 50 hours. Depending on the material, the exact time periods can be adapted to the practical requirements.
- the time for sintering or tempering can be greatly shortened, for example, for periods of 5 minutes to 5 hours, preferably 10 minutes to 1 hour. Compared to the usual values of 10 hours for sintering and 50 hours for annealing, this results in an extreme time advantage.
- the sintering / tempering causes the grain boundaries to melt, so that the material continues to densify.
- stage c) By melting and rapid cooling in stage b), the time duration for stage c) can thus be considerably reduced. This also enables continuous production of the thermomagnetic materials.
- the magnetocaloric materials of the invention may be used in any suitable applications. For example, they are used in coolers, heat exchangers or generators. Particularly preferred is the use in refrigerators.
- Polycrystalline MnCoGe-type samples were prepared by arc melting from stoichiometric amounts of the pure elements. To obtain a homogeneous phase, the cast samples were annealed for 5 days at 500 ° C or 800 ° C under an argon atmosphere of 500 mbar and then quenched in water at room temperature. The crystal structure was determined by X-ray scattering on a powder sample at room temperature. The DC magnetization was determined in a quantum design MPMS2-type squid magnetometer, operating in fields of up to 5 T and in a temperature range of 5 to 400 K.
- FIG. 1 shows the temperature dependence of the magnetization of MnCoGe 0.98 , Mn 0.9 Fe 0.1 CoGe and MnCo 0.9 Cu 0.1 Ge, determined at a magnetic field of 0.1 T (square, circle or triangle). Only the middle sample was annealed.
- the values for the Curie temperature for MnCoGe 0.98 , Mn 0.9 Fe 0.1 CoGe and MnCo 0.9 Cu 0.1 Ge are 325 K, 292 K and 263 K. A thermal hysteresis is observed in the transition from ferromagnetic observed to the paramagnetic state, corresponding to a first order magnetic transition.
- FIG. 2 shows X-ray structure patterns of MnCoGe 0.98 , Mn 0.9 Fe 0.1 CoGe and MnCo 0.9 Cu 0.1 Ge, determined at room temperature. For the sample whose critical temperature is well below room temperature, only the contribution of a single phase of the Ni 2 In type is observed since the measurement temperature is above the critical temperature. Intensity is plotted in arbitrary units.
- Table 2 shows the changes in order temperature (T c ), thermal hysteresis ( ⁇ Thys), change in magnetic entropy (- ⁇ Sm) and magnetic moment for MnCoGeB x compounds annealed at 850 ° C.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Power Engineering (AREA)
- Hard Magnetic Materials (AREA)
- Powder Metallurgy (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10744924.1A EP2467858B1 (de) | 2009-08-18 | 2010-08-17 | Polykristalline magnetokalorische materialien |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09168051 | 2009-08-18 | ||
| PCT/EP2010/061962 WO2011020826A1 (de) | 2009-08-18 | 2010-08-17 | Polykristalline magnetokalorische materialien |
| EP10744924.1A EP2467858B1 (de) | 2009-08-18 | 2010-08-17 | Polykristalline magnetokalorische materialien |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2467858A1 EP2467858A1 (de) | 2012-06-27 |
| EP2467858B1 true EP2467858B1 (de) | 2015-02-18 |
Family
ID=42734573
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10744924.1A Not-in-force EP2467858B1 (de) | 2009-08-18 | 2010-08-17 | Polykristalline magnetokalorische materialien |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20110041513A1 (enExample) |
| EP (1) | EP2467858B1 (enExample) |
| JP (1) | JP5887599B2 (enExample) |
| KR (1) | KR20120054637A (enExample) |
| CN (1) | CN102576587B (enExample) |
| BR (1) | BR112012003818A2 (enExample) |
| CA (1) | CA2771669A1 (enExample) |
| RU (1) | RU2012110126A (enExample) |
| TW (1) | TW201113911A (enExample) |
| WO (1) | WO2011020826A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20130112600A (ko) * | 2012-04-04 | 2013-10-14 | 삼성전자주식회사 | 붕소-도핑된 전이금속 프닉타이드계 자기열효과물질 제조방법 |
| US9255343B2 (en) | 2013-03-08 | 2016-02-09 | Ut-Battelle, Llc | Iron-based composition for magnetocaloric effect (MCE) applications and method of making a single crystal |
| CN103611896B (zh) * | 2013-12-04 | 2016-03-30 | 南昌航空大学 | 一种通过电弧熔炼和熔体快淬制备MnCoGe基和MnNiGe基合金薄带的方法 |
| US9941037B2 (en) * | 2014-01-06 | 2018-04-10 | Instituto Potosino De Investigacion Cientifica y Tecnologica A.C. | Magnetocaloric material based on NdPrFe17 with improved properties |
| ES2940470T3 (es) * | 2014-07-18 | 2023-05-08 | Board Of Supervisors Louisiana State Univ And Agricultural College | Aleaciones multicalóricas de MnNiSi |
| CN105390223B (zh) * | 2015-10-28 | 2018-08-28 | 上海电力学院 | 一种室温磁制冷合金材料及制备方法 |
| WO2018011189A1 (en) * | 2016-07-11 | 2018-01-18 | Basf Se | Magnetocaloric regenerators comprising materials containing cobalt, manganese, boron and carbon |
| CN110468303B (zh) * | 2019-07-30 | 2020-05-22 | 华南理工大学 | 一种医用磁热疗铜镍合金及其制备方法 |
| CN112430757A (zh) * | 2020-10-19 | 2021-03-02 | 北京工业大学 | 一种可用作磁制冷材料的MnCoGe基磁性合金 |
| GB2628175A (en) * | 2023-03-17 | 2024-09-18 | Spirit Aerosys Inc | Composite manufacturing method and apparatus |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US428057A (en) | 1890-05-13 | Nikola Tesla | Pyromagneto-Electric Generator | |
| US3844775A (en) * | 1972-11-24 | 1974-10-29 | Du Pont | Polynary germanides and silicides |
| JPS5463779A (en) * | 1977-10-29 | 1979-05-22 | Nippon Chemical Ind | Signal thansmission means for surveying instrument |
| NL1018668C2 (nl) * | 2001-07-31 | 2003-02-03 | Stichting Tech Wetenschapp | Materiaal geschikt voor magnetische koeling, werkwijze voor het bereiden ervan en toepassing van het materiaal. |
| JP4663328B2 (ja) * | 2003-01-29 | 2011-04-06 | スティッチング ヴォール デ テクニッシェ ヴェッテンシャッペン | 冷却容量を有する磁気材料、当該材料の製造方法および当該材料の使用方法 |
| CA2721621A1 (en) * | 2008-04-28 | 2009-11-05 | Technology Foundation Stw | Method for producing metal-based materials for magnetic cooling or heat pumps |
| CN101555563B (zh) * | 2009-04-30 | 2011-08-31 | 上海大学 | 低磁场下具有巨磁热效应的Gd5Si2-xGe2-xZn2x和Gd5Si2-yGe2Zny合金 |
-
2010
- 2010-08-09 US US12/852,750 patent/US20110041513A1/en not_active Abandoned
- 2010-08-10 TW TW099126669A patent/TW201113911A/zh unknown
- 2010-08-17 JP JP2012525157A patent/JP5887599B2/ja not_active Expired - Fee Related
- 2010-08-17 KR KR1020127006821A patent/KR20120054637A/ko not_active Abandoned
- 2010-08-17 BR BR112012003818A patent/BR112012003818A2/pt not_active IP Right Cessation
- 2010-08-17 CN CN201080046164.8A patent/CN102576587B/zh not_active Expired - Fee Related
- 2010-08-17 EP EP10744924.1A patent/EP2467858B1/de not_active Not-in-force
- 2010-08-17 RU RU2012110126/07A patent/RU2012110126A/ru not_active Application Discontinuation
- 2010-08-17 WO PCT/EP2010/061962 patent/WO2011020826A1/de not_active Ceased
- 2010-08-17 CA CA2771669A patent/CA2771669A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011020826A1 (de) | 2011-02-24 |
| JP5887599B2 (ja) | 2016-03-16 |
| CN102576587B (zh) | 2015-11-25 |
| KR20120054637A (ko) | 2012-05-30 |
| BR112012003818A2 (pt) | 2016-03-22 |
| EP2467858A1 (de) | 2012-06-27 |
| CN102576587A (zh) | 2012-07-11 |
| RU2012110126A (ru) | 2013-09-27 |
| TW201113911A (en) | 2011-04-16 |
| JP2013502510A (ja) | 2013-01-24 |
| CA2771669A1 (en) | 2011-02-24 |
| US20110041513A1 (en) | 2011-02-24 |
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